A Pediatric Acute Promyelocytic Leukemia With a Rare Karyotype of ider(17)(q10)t(15;17) and Favorable Outcome: A Case Report

Acute promyelocytic leukemia (APL) is a specific malignant hematological disorder with a diagnostic hallmark of chromosome translocation t(15;17)(q22;q21). As a very rare secondary cytogenetic aberration in pediatric APL, ider(17q) (q10)t(15;17) was suggested to be a poor prognostic factor based on...

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Detalles Bibliográficos
Autores principales: He, Yanli, Wang, Ping, Liang, Kaiwei, Chen, Xiangjun, Du, Wen, Li, Juan, Hu, Yanjie, Bai, Yan, Liu, Wei, Li, Xiaoqing, Jin, Runming, Zhang, Min, Zheng, Jine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2015
Materias:
4800
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4616798/
https://www.ncbi.nlm.nih.gov/pubmed/26469919
http://dx.doi.org/10.1097/MD.0000000000001778

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4616798/
https://www.ncbi.nlm.nih.gov/pubmed/26469919
http://dx.doi.org/10.1097/MD.0000000000001778

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